digoxin
Generic: digoxin
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
digoxin
Generic Name
digoxin
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
TABLET
Routes
Active Ingredients
digoxin 250 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
0143-1241
Product ID
0143-1241_935f4e33-109c-448c-822c-530145dbbc05
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077002
Listing Expiration
2026-12-31
Marketing Start
2007-10-30
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01431241
Hyphenated Format
0143-1241
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
digoxin (source: ndc)
Generic Name
digoxin (source: ndc)
Application Number
ANDA077002 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 ug/1
Packaging
- 100 TABLET in 1 BOTTLE, PLASTIC (0143-1241-01)
- 1000 TABLET in 1 BOTTLE, PLASTIC (0143-1241-10)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "935f4e33-109c-448c-822c-530145dbbc05", "openfda": {"nui": ["N0000175568", "M0003451"], "upc": ["0301431240103", "0301431241100"], "unii": ["73K4184T59"], "rxcui": ["197604", "197606"], "spl_set_id": ["41c16cff-b03e-405e-a617-d6f45d3ce2bd"], "pharm_class_cs": ["Cardiac Glycosides [CS]"], "pharm_class_epc": ["Cardiac Glycoside [EPC]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0143-1241-01)", "package_ndc": "0143-1241-01", "marketing_start_date": "20071030"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (0143-1241-10)", "package_ndc": "0143-1241-10", "marketing_start_date": "20071030"}], "brand_name": "Digoxin", "product_id": "0143-1241_935f4e33-109c-448c-822c-530145dbbc05", "dosage_form": "TABLET", "pharm_class": ["Cardiac Glycoside [EPC]", "Cardiac Glycosides [CS]"], "product_ndc": "0143-1241", "generic_name": "Digoxin", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Digoxin", "active_ingredients": [{"name": "DIGOXIN", "strength": "250 ug/1"}], "application_number": "ANDA077002", "marketing_category": "ANDA", "marketing_start_date": "20071030", "listing_expiration_date": "20261231"}